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FDA 510(k)

DUAL CURE RELINE MATERIAL

K-Number: K926406 · 1993-03-31

ApplicantDentsply Intl.
Decision Date1993-03-31
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DUAL CURE RELINE MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1993-03-31 under 510(k) number K926406. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL CURE RELINE MATERIAL?

DUAL CURE RELINE MATERIAL is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Dentsply Intl.. The 510(k) number is K926406.

When did DUAL CURE RELINE MATERIAL receive FDA 510(k) clearance?

DUAL CURE RELINE MATERIAL received FDA 510(k) clearance on 1993-03-31, under 510(k) number K926406.

Who is the listed applicant for DUAL CURE RELINE MATERIAL?

The FDA 510(k) record lists Dentsply Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUAL CURE RELINE MATERIAL?

The FDA product code for DUAL CURE RELINE MATERIAL is EBI.

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Related Devices (Code: EBI)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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